[Remote] Associate Clinical Data Reviewer at Clairo

Costa Rica

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Clinical Trials, Healthcare TechnologyIndustries

Requirements

Candidates should possess a Bachelor's degree, preferably in a relevant field, and have at least one year of experience in the pharmaceutical industry or a similar setting. Strong problem-solving, organizational skills, and high attention to detail are essential. The ability to manage multiple tasks concurrently, excellent communication skills, and fluency in English are also required.

Responsibilities

The Associate Clinical Data Reviewer will perform manual data review for Clinical Data Management customers, ensuring data accuracy. This includes issuing queries based on study requirements, participating in project team meetings, generating database metrics and reports, and conducting user acceptance testing. Responsibilities also involve adhering to Clinical Data Management processes, standards, and SOPs, and contributing to team efforts by resolving issues and exploring opportunities for process improvement.

Skills

Data cleaning

Transfer QC

Posting

Query issuance

Database review

User acceptance testing

Problem-solving

Organizational skills

Attention to detail

Time management

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters

1972Year Founded

$29.9MTotal Funding

GROWTH_EQUITY_VCCompany Stage

Biotechnology, HealthcareIndustries

5,001-10,000Employees

Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.

The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.

AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.

The company has nearly 50 years of experience in clinical trial technology solutions.

Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.

The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.

Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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